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The National Lung Matrix Trial: translating the biology of stratification in advanced non-small-cell lung cancer
Authors
A Eyre-Walker
A Gelman
+83 more
AE Locke
Allan F. McRae
AM Hancock
Andres Metspalu
Angli Xue
AR Wood
B Bulik-Sullivan
C Fuchsberger
C Sudlow
CC Chang
Chloe X. Yap
CL Hyde
Cross-Disorder Group of the Psychiatric Genomics Consortium
D Enard
D Habier
D Speed
D Speed
DG Torgerson
DM Altshuler
DR Nyholt
E Marouli
FR Day
G Davies
G Los Campos de
G Moser
GR Abecasis
Grant W. Montgomery
Greg Gibson
J Gratten
J Kelleher
J Yang
J Yang
J Yang
J Yang
JD Storey
Jian Yang
Jian Zeng
JJ Berg
JK Pritchard
JK Pritchard
JM Smith
Joseph E. Powell
Julia Sidorenko
K Walter
L Koning de
LH Uricchio
Loic Yengo
LR Lloyd-Jones
LR Lloyd-Jones
Luke R. Lloyd-Jones
M Konarzewski
Matthew R. Robinson
MC Turchin
MH Moor de
MR Robinson
N Mancuso
Naomi R. Wray
P Wass
Peter M. Visscher
PF Palamara
PM Visscher
PM Visscher
PW Messer
RD Hernandez
RL Fernando
RL Fernando
RL Fernando
Ronald de Vlaming
S Gazal
S Gravel
S McCarthy
SH Lee
SH Lee
T Johnson
TA Manolio
Tonu Esko
V Turcot
WG Hill
X Zhou
Y Field
Y Guan
Yang Wu
YB Simons
Publication date
13 September 2015
Publisher
'Oxford University Press (OUP)'
Doi
Abstract
© The Author 2015.Background: The management of NSCLC has been transformed by stratified medicine. The National Lung Matrix Trial (NLMT) is a UK-wide study exploring the activity of rationally selected biomarker/targeted therapy combinations. Patients and methods: The Cancer Research UK (CRUK) Stratified Medicine Programme 2 is undertaking the large volume national molecular pre-screening which integrates with the NLMT. At study initiation, there are eight drugs being used to target 18 molecular cohorts. The aim is to determine whether there is sufficient signal of activity in any drug-biomarker combination to warrant further investigation. A Bayesian adaptive design that gives a more realistic approach to decision making and flexibility to make conclusions without fixing the sample size was chosen. The screening platform is an adaptable 28-gene Nextera next-generation sequencing platform designed by Illumina, covering the range of molecular abnormalities being targeted. The adaptive design allows new biomarker-drug combination cohorts to be incorporated by substantial amendment. The pre-clinical justification for each biomarker-drug combination has been rigorously assessed creating molecular exclusion rules and a trumping strategy in patients harbouring concomitant actionable genetic abnormalities. Discrete routes of pathway activation or inactivation determined by cancer genome aberrations are treated as separate cohorts. Key translational analyses include the deep genomic analysis of pre- and post-treatment biopsies, the establishment of patient-derived xenograft models and longitudinal ctDNA collection, in order to define predictive biomarkers, mechanisms of resistance and early markers of response and relapse. Conclusion: The SMP2 platform will provide large scale genetic screening to inform entry into the NLMT, a trial explicitly aimed at discovering novel actionable cohorts in NSCLC
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